GAS7, growth arrest specific 7, 8522

N. diseases: 23; N. variants: 10
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9913911
rs9913911 		0.925 0.040 17 10127866 intron variant A/G snv 0.32
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 6 2014 2018
dbSNP: rs10852918
rs10852918 		17 9937184 intron variant A/G snv 0.49
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 2 2018 2018
dbSNP: rs11656696
rs11656696 		0.882 0.040 17 10130362 intron variant C/A snv 0.36
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 2 2012 2017
dbSNP: rs11656696
rs11656696 		0.882 0.040 17 10130362 intron variant C/A snv 0.36
CUI: C0021888
Disease: Physiologic Intraocular Pressure
Physiologic Intraocular Pressure 		0.700 1.000 1 2012 2012
dbSNP: rs12150284
rs12150284 		1.000 0.040 17 10127773 intron variant C/A;G;T snv
CUI: C0017601
Disease: Glaucoma
Glaucoma 		Eye Diseases 0.700 1.000 1 2018 2018
dbSNP: rs12150284
rs12150284 		1.000 0.040 17 10127773 intron variant C/A;G;T snv
CUI: C0021888
Disease: Physiologic Intraocular Pressure
Physiologic Intraocular Pressure 		0.700 1.000 1 2012 2012
dbSNP: rs12150284
rs12150284 		1.000 0.040 17 10127773 intron variant C/A;G;T snv
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs17683107
rs17683107 		1.000 0.040 17 9921085 intron variant G/A snv 0.13
CUI: C0566602
Disease: Primary sclerosing cholangitis
Primary sclerosing cholangitis 		Digestive System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2320549
rs2320549 		17 10141230 intron variant A/G;T snv 0.32
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7214058
rs7214058 		1.000 0.040 17 10080017 intron variant T/A;G snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs7214058
rs7214058 		1.000 0.040 17 10080017 intron variant T/A;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs7222232
rs7222232 		17 10033485 intron variant A/C snv 1.3E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7222232
rs7222232 		17 10033485 intron variant A/C snv 1.3E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8071787
rs8071787 		17 10058819 intron variant T/C snv 4.8E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8071787
rs8071787 		17 10058819 intron variant T/C snv 4.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8071787
rs8071787 		17 10058819 intron variant T/C snv 4.8E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8071787
rs8071787 		17 10058819 intron variant T/C snv 4.8E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8071787
rs8071787 		17 10058819 intron variant T/C snv 4.8E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9889528
rs9889528 		17 10132020 intron variant C/T snv 0.30
CUI: C0021888
Disease: Physiologic Intraocular Pressure
Physiologic Intraocular Pressure 		0.700 1.000 1 2012 2012
dbSNP: rs9913911
rs9913911 		0.925 0.040 17 10127866 intron variant A/G snv 0.32
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle 		Eye Diseases 0.700 1.000 1 2018 2018
dbSNP: rs9913911
rs9913911 		0.925 0.040 17 10127866 intron variant A/G snv 0.32
CUI: C0021888
Disease: Physiologic Intraocular Pressure
Physiologic Intraocular Pressure 		0.700 1.000 1 2012 2012
dbSNP: rs9913911
rs9913911 		0.925 0.040 17 10127866 intron variant A/G snv 0.32
CUI: C0017601
Disease: Glaucoma
Glaucoma 		Eye Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11656696
rs11656696 		0.882 0.040 17 10130362 intron variant C/A snv 0.36
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle 		Eye Diseases 0.020 0.500 2 2017 2019
dbSNP: rs11656696
rs11656696 		0.882 0.040 17 10130362 intron variant C/A snv 0.36
CUI: C0017601
Disease: Glaucoma
Glaucoma 		Eye Diseases 0.010 1.000 1 2012 2012
dbSNP: rs11656696
rs11656696 		0.882 0.040 17 10130362 intron variant C/A snv 0.36
CUI: C0595921
Disease: Intraocular pressure disorder
Intraocular pressure disorder 		Eye Diseases 0.010 < 0.001 1 2017 2017